Canonical Allele Identifier: CA200764851

Gene: ABO

Linked Data

• dbSNP Id: rs201070878
• MyVariant Identifiers: chr9:g.136130743_136130744insA (hg19) ; chr9:g.133255356_133255357insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255356_133255357insA , CM000671.2:g.133255356_133255357insA	GRCh38
NC_000009.11:g.136130743_136130744insA , CM000671.1:g.136130743_136130744insA	GRCh37
NC_000009.10:g.135120564_135120565insA	NCBI36
NG_006669.1:g.22311_22312insT
NG_006669.2:g.24859_24860insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1403_1404insT
ENST00000647353.1:n.54-4205_54-4204insT
ENST00000679909.1:c.28+19805_28+19806insT	ENSP00000506089.1:n.28+19805_28+19806insT
ENST00000453660.3:n.1385_1386insT
ENST00000611156.4:c.*309_*310insT	ENSP00000483265.1:n.*309_*310insT
NM_020469.2:c.*309_*310insT	NP_065202.2:n.*309_*310insT
NM_020469.3:c.*309_*310insT	NP_065202.2:n.*309_*310insT